At a glance
ClinicalIndex Comparison RecordN/ACompleted· 32 enrolled
Drug / intervention
Zimmer MotionLoc Screwdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Zimmer® MotionLoc® in Distal Tibia Fractures: An Observational Study
In Brief
An observational study evaluating Zimmer MotionLoc Screw for Distal Tibia Fractures. Completed, enrolled 32 participants across 7 sites in 5 countries.
Detailed Summary
The objective of this observational prospective study is to systematically document the clinical outcomes of Zimmer MotionLoc Screws for Periarticular Locking Plate System applied to distal tibia fracture treatment and confirm safety and performance of the screws.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsDistal Tibia Fractures
CountriesAustralia, Italy, South Korea, United Kingdom, United States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartFeb 2016
First PostedMar 2016
Primary CompletionDec 2019
Study CompletionJan 2020
TodayJul 2026
First PostedMar 23, 2016
Enrollment StartFeb 1, 2016
Primary CompletionDec 5, 2019
Study CompletionJan 15, 2020
TodayJul 2, 2026
Enrollment to primary: 3.8 yearsPosted 10.3 years ago
Interventions
Zimmer MotionLoc Screwdevice
Patients with distal tibia fractures (AO 43-A and C) requiring surgical intervention eligible for locked plating.